Canonical Allele Identifier: CA1328738830

Gene: SLC11A1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.218395121A= , CM000664.2:g.218395121A=	GRCh38
NC_000002.11:g.219259844A= , CM000664.1:g.219259844A=	GRCh37
NC_000002.10:g.218968088A=	NCBI36
NG_012128.1:g.18093A=
NG_030418.1:g.1784A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233202.11:c.*86A= MANE Select	ENSP00000233202.6:n.*86A=
ENST00000233202.10:c.*86A=	ENSP00000233202.6:n.*86A=
ENST00000354352.9:c.*1321A=	ENSP00000346320.5:n.*1321A=
ENST00000465984.5:n.2160+55A=
ENST00000468221.5:n.4866A=
NM_000578.3:c.*86A=	NP_000569.3:n.*86A=
XM_005246793.2:c.*86A=	XP_005246850.1:n.*86A=
XM_005246794.2:c.*86A=	XP_005246851.1:n.*86A=
XM_006712709.2:c.*86A=	XP_006712772.1:n.*86A=
XM_006712710.2:c.*86A=	XP_006712773.1:n.*86A=
XM_006712711.2:c.*86A=	XP_006712774.1:n.*86A=
XM_011511684.1:c.*86A=	XP_011509986.1:n.*86A=
XM_011511685.1:c.*86A=	XP_011509987.1:n.*86A=
XM_005246793.4:c.*86A=	XP_005246850.1:n.*86A=
XM_005246794.4:c.*86A=	XP_005246851.1:n.*86A=
XM_006712709.4:c.*86A=	XP_006712772.1:n.*86A=
XM_006712710.4:c.*86A=	XP_006712773.1:n.*86A=
XM_006712711.4:c.*86A=	XP_006712774.1:n.*86A=
XM_011511684.3:c.*86A=	XP_011509986.1:n.*86A=
XM_011511685.3:c.*86A=	XP_011509987.1:n.*86A=
XM_017004765.2:c.*86A=	XP_016860254.1:n.*86A=
XM_017004766.2:c.*86A=	XP_016860255.1:n.*86A=
XM_017004767.2:c.*86A=	XP_016860256.1:n.*86A=
XR_427107.3:n.2754A=
XR_427108.4:n.3065A=
NM_000578.4:c.*86A= MANE Select	NP_000569.3:n.*86A=